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THJ-018

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
THJ-018
Legal status
Legal status
Identifiers
  • 1-Naphthalenyl(1-pentyl-1H-indazol-3-yl)-methanone
CAS Number
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC23H22N2O
Molar mass342.442 g·mol−1
3D model (JSmol)
  • O=C(C1=NN(CCCCC)C2=C1C=CC=C2)C3=C4C(C=CC=C4)=CC=C3
  • InChI=1S/C23H22N2O/c1-2-3-8-16-25-21-15-7-6-13-20(21)22(24-25)23(26)19-14-9-11-17-10-4-5-12-18(17)19/h4-7,9-15H,2-3,8,16H2,1H3
  • Key:VAKGBPSFDNTMDJ-UHFFFAOYSA-N

THJ-018 (SGT-17) is asynthetic cannabinoid that is theindazole analogue ofJWH-018 and has been sold online as adesigner drug.[1][2]

Pharmacology

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THJ-018 acts as afull agonist with abinding affinity of 5.84 nM atCB1 and 4.57 nM atCB2cannabinoid receptors.[3]

Legality

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THJ-018 is anAnlage II controlled drug in Germany.[4] It is also banned in Sweden.[5]

See also

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References

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  1. ^"THJ-018". Cayman Chemical. Retrieved9 July 2015.
  2. ^Diao X, Wohlfarth A, Pang S, Scheidweiler KB, Huestis MA (January 2016)."High-Resolution Mass Spectrometry for Characterizing the Metabolism of Synthetic Cannabinoid THJ-018 and Its 5-Fluoro Analog THJ-2201 after Incubation in Human Hepatocytes".Clinical Chemistry.62 (1):157–69.doi:10.1373/clinchem.2015.243535.PMID 26430074.
  3. ^Hess C, Schoeder CT, Pillaiyar T, Madea B, Müller CE (2016)."Pharmacological evaluation of synthetic cannabinoids identified as constituents of spice".Forensic Toxicology.34 (2):329–343.doi:10.1007/s11419-016-0320-2.PMC 4929166.PMID 27429655.
  4. ^"Gesetz über den Verkehr mit Betäubungsmitteln (Betäubungsmittelgesetz - BtMG) Anlage II (zu § 1 Abs. 1) (verkehrsfähige, aber nicht verschreibungsfähige Betäubungsmittel)" (in German). Retrieved9 July 2015.
  5. ^"Cannabinoider föreslås bli klassade som hälsofarlig vara" (in Swedish). Folkhälsomyndigheten. Retrieved9 July 2015.
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